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A.N.U. B.PHARMACY SYLLABUS (WITH EFFECT FROM 2008 - 09 ACADEMIC YEAR)
III/IV B.PHARMACY (5th Semester)
501 PHARMACEUTICAL CHEMISTRY-IV (MEDICINALII)
(Theory) (75 hrs.)
Unit : 01
Quantitative structure activity relationship (QSAR) studies, basic concepts of
computer aided drug design, different drug design approaches, basic
concepts of combinatorial synthesis.
Unit : 02
General Anaesthetics : Introduction, classification, mechanism of action,
synthesis and therapeutic uses of halothane, ketamine, methohexital.
Local Anaesthetics : Introduction, chemical classification, ideal requirements,
mode of action, SAR, structures of important local anaesthetics, metabolism
and synthesis of benzocaine, procaine, lidocaine, tetracaine and cinchocaine.
Hypnotics and Sedatives – SAR of barbiturates, synthesis, metabolism and
therapeutic uses of phenobarbital, amylobarbital, pentobarbital, cyclobarbitone
calcium, thiopental, hexobarbital. chlordiazepoxide, diazepam, alprazolam.
Anti-psychotics – SAR of phenothiazines, synthesis and therapaeutic uses of
promethazine, Prochlorperazine, Fluphenazine, chlorpromazine, haloperidol,
clozapine, oxypentine.
Anti– depressants: Synthesis and therapaeutic uses of amitryptaline, doxepine,
iproniazid, isocarboxizide, trazodone, fluoxetin
Anti – Anxietyagents : Synthesis and therapaeutic uses of nitrazepam,
lorazepam, prazepam
Anti-epileptics – Synthesis and therapaeutic uses of phenytoin, valproic acid,
carbamazepine, ethosuximide.
Unit : 03
Drugs affecting adrenergic mechanism : Adrenergic receptors, biosynthesis of
catecholamines, chemical classification along with structures, S.A.R of
adrenergic drugs, adrenergic agonists, adrenergic blockers. Synthesis
and therapeutic uses of phenylephrine, ephedrine, naphazoline, terbutaline,
dopamine, amphetamine, phenoxybenzamine, propranolol, metaprolol, atenolol,
tolazoline.
Drugs affecting cholinergic mechanism: Introduction, SAR, cholinergic
receptors, study of cholinergic agonists, indirectly acting cholinergic agonists,
cholinergic blocking agents, neuromuscular blocking agents. Synthesis and
therapeutic uses of methacholine, carbachol, neostigmine, pralidoxime,
propantheline, dicyclamine, tropicamide, atropine, bipyridine.
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A.N.U. B.PHARMACY SYLLABUS (WITH EFFECT FROM 2008 - 09 ACADEMIC YEAR)
Unit : 04
Cardiovascular Agents: Introduction, classification, mechanism of action of
antianginal agents, calcium channel blockers, Anti-arrhythmic drugs,
antihypertensive agents, antihyperlipidemic agents and anticoagulants.
Synthesis and therapeutic uses of methyldopa, amlodipine, clonidine,
hydralazine, verapamil, clofibrate, dicoumorol, warfarin
Hypoglycaemics : General account on pancreatic malfunctions. chemical
classification, S.A.R of hypoglycemics, Insulin preparations, a brief account
on statin antidiabetics – phenformin, glipizide, chlopropamide, including
a brief account on PPARγ inhibitors, meglitinide analogues, α-glucosidase
inhibitors–Acarbose, miglitol. A brief account on thyroid and antithyroid
drugs.
Unit : 05
Opoid Analgesics : Classification along with structures, mechanism of action,
S.A.R of opioid analgesics, mixed agonists and mixed antagonists, central and
peripheral acting anti tussive agents. Structure and therapeutic uses of
morphine, codeine, diacetylmorphine, nalorphine, levalophan, noscapine,
dextromethorphan.
NSAIDS (Non-steroidal anti-inflamatory agents) : Introduction and types
of pain and inflammation. Synthesis, metabolism and therapeutic uses of
aspirin, paracetamol, ibuprofen, mefenamic acid, diclofenac, piroxicam.
A brief account on Cox-2 inhibitors.
Unit : 06
DIURETICS : Introduction, chemical classification along with structures,
mechanism of action, S.A.R, metabolism and synthesis of acetazolamide,
benzthiazide, furosemide, ethacrynic acid chlorthiazide, hydrochlorthiazide
and amiloride.
Antihistaminic agents : Introduction, histamine receptors, biosynthesis of
histamine, study of H1 and H2 antagonists. Chemical classification along
with structures, mechanism of action, S.A.R, of antihistamines. Synthesis
and metabolism of diphenhydramine, pyrilamine, mepyramine, cyclizine
pheninramine, promethazine, antazoline, astimizole, cetrizine, cimetidine.
Diagnostic agents : Introduction, structures and therapeutic uses of some
important organic compounds as diagnostic agents. Synthesis of iopanoic
acid, fluorescein, diatriazoic acid and metyrapone
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A.N.U. B.PHARMACY SYLLABUS (WITH EFFECT FROM 2008 - 09 ACADEMIC YEAR)
III/IV B.PHARMACY (5th Semester)
502 PHARMACEUTICAL CHEMISTRYIV
(MEDICINAL-II) (Practicals) (75 hrs.)
01*. Assay of indomethacin capsules – I.P.
02*. Assay of glipizide/frusemide tablets – I.P.
03*. Assay of ibuprofen suspension – I.P.
04*. Assay of paracetamol elixir/tablet – I.P.
05. Assay of ascorbic acid tablets – I.P.
06*. Assay of salicylic acid ointment – I.P.
07*. Assay of aminophylline injection - I.P.
08. Assay of metronidazole tablets – I.P.
09*. Synthesis of benzil from benzoin
10. Synthesis of benzillic acid from benzil
11. Synthesis of 7-hydroxy 4-methyl coumarin
12. Synthesis of benzimidazole
13*. Synthesis of benzocaine
14*. Synthesis of benzotriazole
15. Synthesis of aspirin
16*. Synthesis of phenytoin (5, 5’ – diphenyl hydantoin)
17. Synthesis of sulphanilamide.
TEST BOOKS
1. Text book of Medicinal Chemistry by William O. Foye, Lea Febiger,
Philadelphia. Wilson & Giswold’s Text book of organic Medicinal Chemistry
th
and pharmaceutical chemistry by JH Block & JM Beale (Eds), 11 Ed, Lipcott,
Raven, Philadelphia, 2004.
2. D. Abraham (Ed), Burger Medicinal chemistry ad Drug discovery, Vol. 1 & 2.
John Wiley & Sons, New York 2003, 6th Ed.
3. Lippincott Williams and Wilkins: Remington Pharmaceutical Sciences;
20th Edition.
4. Bentley and Driver’s Textbook of Pharmaceutical Chemistry Ed: l. M.
Atherden. Oxford University Press, Delhi.
5. B.N. Lads, MG.Mandel and F.I. way, Fundamentals of drug metabolism &
disposition, William & welking co, Baltimore USA.
6. Hansch, Comprehensive medicinal chemistry, Vol 1 – 6 Elsevier pergmon
press, Oxford
7. Rama Rao Nadendla, Principles of Organic Medicinal chemistry, Vol-I,
New-Age International Publishers Pvt., limited, New Delhi, 2005
8. Daniel lednicer, Strategies For Organic Drug Synthesis And Design, John
Wiley, N. Y. 1998.
9. D. Lednicer, Organic drug synthesis, Vol, 1 – 6, J.Wiley N.Y.
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A.N.U. B.PHARMACY SYLLABUS (WITH EFFECT FROM 2008 - 09 ACADEMIC YEAR)
th
III/IV B.PHARMACY (5 Semester)
MODEL QUESTION PAPER
501 PHARMACEUTICAL CHEMISTRY-IV (MEDICINAL-II) (Theory)
Time : 3 hours Max.Marks : 80
SECTION-A
Answer any four questions (4 X 10 = 40 marks)
1. Add a note on different drug design approaches. Give a detailed
account of computer aided drug design.
2. Classify sedatives and hypnotics with suitable examples. Write
the SAR and mode of action of Barbiturates.
3. Outline the chemical classification of adrenergic drugs. Discuss
their mode of action and SAR.
4. What are oral hypoglycemic agents ? Classify them with examples
and write their mode of action.
5. Classify the non-steroidal anti inflammatory agents with examples and
discuss their mode of action ? How do you synthesize diclofenac and
piroxicom ?
6. Classify H1 antagonists with examples ? Discuss the SAR and
mechanism of action of these drugs.
SECTION - B
Answer any TEN questions (10 X 4 = 40 marks)
7. Write short notes on Free Wilson analysis
8. Short notes on descriptors used in QSAR
9. Outline the synthesis and therapeutic uses of phenytoin.
10. Mechanism of action of MAO inhibitors.
11. Short notes on cholinergic receptors.
12. Give the synthesis and mechanism of propantheline.
13. Write short notes on antianginal agents.
14. Outline the synthesis of clonidine
15. Discuss the mode of action of opioid analgesics
16. Short notes on opioid antagonists
17. Write the SAR and mode of action of thiazide diuretics.
18. Add a note on synthesis and metabolism of cetrizine.
th
III/IV B.PHARMACY (5 Semester)
MODEL QUESTION PAPER (Practicals)
502 PHARMACEUTICAL CHEMISTRY-IV (MEDICINAL-II)
Time : 4 hours Max.Marks : 80
1. Synopsis : 10 Marks
2*. Major Experiment : 35 Marks
3. Minor Experiment : 20 Marks
4. Viva-Voce : 15 Marks
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Total: 80 Marks
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